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Amlodipine and Atorvastatin

NDC 66993-264 · Prasco Laboratories

Generic nameAmlodipine and Atorvastatin
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)AMLODIPINE BESYLATE, ATORVASTATIN CALCIUM TRIHYDRATE
Strength2.5; 20 mg/1; mg/1
Pharmacologic classCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryNDA AUTHORIZED GENERIC

Packages

66993-264-30 — 30 TABLET, COATED in 1 BOTTLE (66993-264-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-834 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-835 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-836 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-837 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-838 — Amlodipine, Valsartan and Hydrochlorothiazide, 65862-854 — Amlodipine and Olmesartan Medoxomil, 65862-855 — Amlodipine and Olmesartan Medoxomil, 65862-856 — Amlodipine and Olmesartan Medoxomil, 65862-857 — Amlodipine and Olmesartan Medoxomil, 66993-263 — Amlodipine and Atorvastatin, 66993-265 — Amlodipine and Atorvastatin, 66993-266 — Amlodipine and Atorvastatin, 66993-267 — Amlodipine and Atorvastatin, 66993-268 — Amlodipine and Atorvastatin, 66993-269 — Amlodipine and Atorvastatin, 66993-270 — Amlodipine and Atorvastatin, 66993-271 — Amlodipine and Atorvastatin, 66993-272 — Amlodipine and Atorvastatin, 66993-273 — Amlodipine and Atorvastatin, 67046-0328 — Amlodipine besylate, +824 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.